Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
PBRM1

Cell type

Cell type Class
Kidney
Cell type
NCC2112
NA
NA

Attributes by original data submitter

Sample

source_name
Cancer cell line
source
NCC2112 (in house derived cancer cell line)
protein
PBRM1
treatment
empty vector
chip antibody
PBRM1(Bethyl, A301-591A, lot3)

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For each protein of interest, approximately 2x107 cells were cross-linked with 1% formaldehyde for 10 min at room temperature, and stopped by adding glycine to a final concentration of 0.2M. Chromatin was extracted and sonicated to ~500bp (Vibra cell, SONICS). The total volume of immunoprecipitation was 2 ml and the amount of antibody used was 20 µg. The input DNA was precleared with protein G Dynabeads (LifeTechnologies) for 2 hours at 4°C and then incubated with antibodies overnight at 4°C. Protein G beads were added the following day and mixture was nutated for 3 hours at 4°C. The beads were washed 6 times with wash buffer at room temperature. At least 10 ng of the amplified DNA was used with NEBNext ChIP-Seq library prep reagent set (NEB). Each library was sequenced to an average depth of 30-50 million reads on HiSeq2500 or HiSeq4000.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
7879125
Reads aligned (%)
92.6
Duplicates removed (%)
66.0
Number of peaks
542 (qval < 1E-05)

hg19

Number of total reads
7879125
Reads aligned (%)
91.9
Duplicates removed (%)
67.4
Number of peaks
566 (qval < 1E-05)

Base call quality data from DBCLS SRA